ClinVar Miner

List of variants reported as pathogenic for Autosomal recessive ataxia due to ubiquinone deficiency by GeneReviews

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000001.10:g.227150977_227195656del44680

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